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The Zn-MnO2 battery: The influence of aqueous LiOH and KOH electrolytes on the intercalation mechanism

机译:Zn-MnO2电池:LiOH和KOH电解质水溶液对嵌入机理的影响

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Intercalation chemistry of the zinc-manganese dioxide (Zn-MnO2) electrochemical cell aiming at the development of aqueous rechargeable batteries is presented. This study includes electrochemical characterization of MnO2 in saturated aqueous lithium hydroxide (LiOH) and potassium hydroxide (KOH) electrolytes. The lithium insertion into MnO2 results in the formation of LixMnO2. The reversible deintercalation process prevails in the presence of LiOH electrolyte. Rather than the usual protonation (H+) which is apparent in the literature while using KOH electrolyte, in this work, K+ ion insertion into MnO2 is observed. However, the K+ ion insertion is found to be irreversible. The intercalation mechanism is confirmed using various techniques to characterize the discharged MnO2 cathode in LiOH and KOH electrolytes. The influence of small amounts of Bi2O3 (bismuth oxide) additive on the discharge behavior of MnO2 is also discussed.
机译:提出了针对水性可充电电池发展的锌-二氧化锰(Zn-MnO2)电化学电池的插层化学。这项研究包括在饱和氢氧化锂(LiOH)和氢氧化钾(KOH)电解质中MnO2的电化学表征。锂插入MnO2会形成LixMnO2。在LiOH电解质的存在下,可逆的脱嵌过程占主导。在这项工作中,观察到的是K +离子插入MnO2中,而不是使用KOH电解质时在文献中显而易见的常规质子化(H +)。然而,发现K +离子的插入是不可逆的。使用各种技术可以确定嵌入机理,以表征LiOH和KOH电解质中放电的MnO2阴极。还讨论了少量Bi2O3(氧化铋)添加剂对MnO2放电行为的影响。

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